The following data is part of a premarket notification filed by Daig Corp. with the FDA for Daig Obturator, Catheter Introducer.
| Device ID | K884494 |
| 510k Number | K884494 |
| Device Name: | DAIG OBTURATOR, CATHETER INTRODUCER |
| Classification | Introducer, Catheter |
| Applicant | DAIG CORP. 14901 DEVEAU PLACE Minnetonka, MN 55345 -2126 |
| Contact | J Fleischhacker |
| Correspondent | J Fleischhacker DAIG CORP. 14901 DEVEAU PLACE Minnetonka, MN 55345 -2126 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-10-25 |
| Decision Date | 1989-02-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 15415067009460 | K884494 | 000 |
| 15415067009316 | K884494 | 000 |
| 15414734053836 | K884494 | 000 |
| 15414734053812 | K884494 | 000 |
| 15414734053799 | K884494 | 000 |
| 15414734053775 | K884494 | 000 |
| 15414734053751 | K884494 | 000 |
| 15414734026595 | K884494 | 000 |
| 15414734026564 | K884494 | 000 |
| 15415067009323 | K884494 | 000 |
| 15415067009330 | K884494 | 000 |
| 15415067009354 | K884494 | 000 |
| 15415067009446 | K884494 | 000 |
| 15415067009439 | K884494 | 000 |
| 15415067009422 | K884494 | 000 |
| 15415067009415 | K884494 | 000 |
| 15415067009408 | K884494 | 000 |
| 15415067009385 | K884494 | 000 |
| 15415067009378 | K884494 | 000 |
| 15415067009361 | K884494 | 000 |
| 15414734022498 | K884494 | 000 |